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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AMBRISENTAN Cause Device issue? 113 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 113 reports of Device issue have been filed in association with AMBRISENTAN (AMBRISENTAN). This represents 0.1% of all adverse event reports for AMBRISENTAN.

113
Reports of Device issue with AMBRISENTAN
0.1%
of all AMBRISENTAN reports
5
Deaths
66
Hospitalizations

How Dangerous Is Device issue From AMBRISENTAN?

Of the 113 reports, 5 (4.4%) resulted in death, 66 (58.4%) required hospitalization, and 4 (3.5%) were considered life-threatening.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AMBRISENTAN. However, 113 reports have been filed with the FAERS database.

What Other Side Effects Does AMBRISENTAN Cause?

Dyspnoea (13,367) Death (7,497) Headache (7,325) Pneumonia (4,693) Dizziness (4,561) Fatigue (4,436) Diarrhoea (4,312) Nausea (3,986) Fluid retention (3,927) Malaise (3,839)

What Other Drugs Cause Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which AMBRISENTAN Alternatives Have Lower Device issue Risk?

AMBRISENTAN vs AMBROSIA ARTEMISIIFOLIA POLLEN AMBRISENTAN vs AMBROXOL AMBRISENTAN vs AMDINOCILLIN PIVOXIL AMBRISENTAN vs AMG-510 AMBRISENTAN vs AMIFAMPRIDINE

Related Pages

AMBRISENTAN Full Profile All Device issue Reports All Drugs Causing Device issue AMBRISENTAN Demographics